A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626587



Internal ID7013419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61940264..61941576hg38UCSC Ensembl
Innerchr11:61940294..61941547hg38UCSC Ensembl
Outerchr11:61940235..61941606hg38UCSC Ensembl
chr11:61707736..61709048hg19UCSC Ensembl
Innerchr11:61707766..61709019hg19UCSC Ensembl
Outerchr11:61707707..61709078hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381313
hg191313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14178523
SamplesHG02150
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626587
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer